of diseases. For example, inducing cancer cells from the aggressive and unrestricted growth state to a senescent state can limit their proliferation and reduce their resistance to treatments, [2] which can be realized by intracellular catalytic reduction of β-nicotinamide adenine dinucleotide (NAD + ). [3] However, it remains a challenge to realize highly efficient intracellular catalysis of nanocatalysts in the complex tumor microenvironment.Catalytic reaction is accompanied by electron transfer, and regulating the electronic structure of the catalyst has been an efficient way to improve the catalytic activity. [4] Heterostructures are superior in electron regulation owing to the spontaneous charge rearrangement at the interface driven by the difference in work function and Fermi level between materials, [5] thereby influencing the catalytic activities. [6] Moreover, the electron transfer tendency in heterostructures can be managed by integrating materials with different work functions. [7] By integrating Au nanoparticles with higher work function (work function = 5.27 eV) and Fe 2 C nanoparticles (work function = 4.89 eV) into a Janus-like Au-Fe 2 C heterostructure, we recently demonstrated a catalytic radiotherapy owing to enriched charges of Au. [8] However, its efficiency is insufficient. The key to further increasing the catalytic activity lies
Intracellular catalytic reactions can tailor tumor cell plasticity toward highefficiency treatments, but the application is hindered by the low efficiency of intracellular catalysis.Here, a magneto-electronic approach is developed for efficient intracellular catalysis by inducing eddy currents of FePt-FeC heterostructures in mild alternating magnetic fields (frequency of f = 96 kHz and amplitude of B ≤ 70 mT). Finite element simulation shows a high density of induced charges gathering at the interface of FePt-FeC heterostructure in the alternating magnetic field. As a result, the concentration of an essential coenzyme-β-nicotinamide adenine dinucleotide-in cancer cells is significantly reduced by the enhanced catalytic hydrogenation reaction of FePt-FeC heterostructures under alternating magnetic stimulation, leading to over 80% of senescent cancer cells-a vulnerable phenotype that facilitates further treatment. It is further demonstrated that senescent cancer cells can be efficiently killed by the chemodynamic therapy based on the enhanced Fentonlike reaction. By promoting intracellular catalytic reactions in tumors, this approach may enable precise catalytic tumor treatment.